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Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. We are PCI. Our investment is in People who make an impact, drive progress and create a better tomorrow. Our…
The QA Specialist II provides on-the-floor quality oversight for manufacturing and visual inspection activities in a GMP facility. This role involves ensuring compliance with regulatory standards, reviewing batch records, and managing quality investigations for drug product production.
The QA Operations Specialist II provides on-the-floor quality oversight for manufacturing and visual inspection activities in a GMP facility. This role involves batch record review, compliance monitoring, and supporting investigations to ensure adherence to regulatory standards.
Perform real-time GMP quality assurance for biopharma manufacturing, including floor oversight, batch record review, AQL inspections, and issue resolution to ensure regulatory compliance and patient safety.
Design, implement, and maintain a global enterprise network using Cisco technologies, SD-WAN, and advanced routing/switching to ensure high availability and security across multiple continents.
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